Hereditary Disorders tests in Dubai & UAE

Compare available Hereditary Disorders tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Hereditary Disorders test prices

Showing 1–3 of 3 matching tests.

Hereditary Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5176 Ectodermal Dysplasia, Hypohidrotic, X-Linked (EDA) Gene Genetic Test This genetic test identifies pathogenic variants in the EDA gene responsible for X-linked hypohidrotic ectodermal dysplasia (XLHED). It sequences the entire coding region and splic...	Peripheral Whole Blood (or Buccal Swab for Infants)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the EDA gene", "Single-nucleotide variants", "Small insertions/deletions", "Larger structural rearrangements"] Parameters [] Preparation ["No fasting is necessary", "Stay well hydrated", "Provide phlebotomist with a complete list of current medications and relevant medical history"] Indications ["Patients presenting with clinical signs of hypohidrotic ectodermal dysplasia", "Individuals with a confirmed family history of XLHED"] Measurement technique Confirm with laboratory Codes LOINC: 81321-2 ICD-10: Q82.4 Clinical summary This genetic test identifies pathogenic variants in the EDA gene responsible for X-linked hypohidrotic ectodermal dysplasia (XLHED). It sequences the entire coding region and splice junctions of the EDA gene.
TEST-2178 FBN1 Gene (Weill-Marchesani Syndrome, Dominant Type 2) Next-Generation Sequencing Genetic Test This test analyzes the FBN1 gene for pathogenic variants associated with Weill-Marchesani syndrome type 2.	Peripheral Whole Blood (EDTA), Extracted DNA, or Buccal Swab	10–14 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FBN1 gene sequence", "Copy Number Variations (CNVs) in FBN1"] Parameters [] Preparation ["Pre-test genetic counseling session required", "No fasting required", "Avoid heparin-based anticoagulants"] Indications ["Clinical suspicion of Weill-Marchesani syndrome type 2", "Family history of Weill-Marchesani syndrome", "Need for genetic confirmation for management and counseling"] Measurement technique Confirm with laboratory Codes LOINC: 74891-3 ICD-10: Q87.1 Clinical summary This test analyzes the FBN1 gene for pathogenic variants associated with Weill-Marchesani syndrome type 2.
TEST-5517 WFS1 Gene Wolfram-like Syndrome Autosomal Dominant Genetic Test This test evaluates the WFS1 gene for mutations associated with autosomal dominant Wolfram-like syndrome.	Peripheral whole blood (EDTA) or FTA card (dried blood spot)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["WFS1 gene mutations", "Copy Number Variants (CNVs) in WFS1"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your physician"] Indications ["Unexplained sensorineural hearing loss", "Optic atrophy", "Early-onset diabetes or diabetes insipidus"] Measurement technique Confirm with laboratory Codes LOINC: 82161-3 ICD-10: E13.8 Clinical summary This test evaluates the WFS1 gene for mutations associated with autosomal dominant Wolfram-like syndrome.

Category overview

Hereditary Disorders: overview

A family history of chronic illnesses or overlapping, unexplained generational symptoms warrants proactive, empowering insights to break the cycle and protect your future health. Integrated into our comprehensive Genetics department, testing for broad Hereditary Disorders evaluates your DNA for a vast spectrum of familial mutations passed down through generations. Utilizing advanced sequencing technology, this expansive molecular profiling helps identify hidden molecular risks long before symptoms escalate, safely guiding your healthcare provider in tailoring highly personalized preventative care, customized medical therapies, and proactive family planning. Recognized for preventative diagnostic excellence across the best diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical accuracy, and incredibly prompt reporting. Take an empowered step toward targeted wellness—book your hereditary disorders testing in UAE, arrange a secure home sample collection, or reach out to our specialized genetic team.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.